Abstract
Silver nanoparticles (AgNPs)‐based nanozyme sensors are gaining attention for rapid on‐site H2O2 detection, which is beneficial to disease diagnosis and environmental monitoring. However, the severe agglomeration of AgNPs on the electrodes significantly reduced electrochemical catalytic activity. In this work, we fabricated N‐doped Ti3C2 MXene (named Ag/N−Ti3C2) deposited with three‐dimensional flower‐like AgNPs to achieve ultrasensitive H2O2 detection. N doping strategy is employed to improve the conductivity of MXene, and the corresponding catalytic activity of Ag/N−Ti3C2 is enhanced by optimizing the growth process and morphology. The Ag/N−Ti3C2/glassy carbon electrode (Ag/N‐Ti3C2/GCE) sensor exhibited a wide H2O2 detection range (0.05–35 mM), a low limit detection (1.53 μM), and 3.1 % relative standard deviation in 50 repeated cyclic voltammetry measurements. The results above indicate that catalytic activity of metal nanozymes could be influenced by the substrate and both materials jointly determine the sensor's performance. As a result, N‐doped MXene is an attractive candidate for biological sensing and other electrocatalytic applications.
Both substrate and nanozyme matter: N‐doped Ti3C2 was prepared by hyperpyrexia carbonization method using dopamine as nitrogen source. Ag nanozymes were then grown onto N−Ti3C2 surface by electrodeposition, showing regular 3D nanoflower structures. The Ag/N−Ti3C2/GCE directly acted as a nanozyme sensor, which exhibited excellent performance towards H2O2 sensing with an ultrahigh sensitivity, low detection limit and wide detection range.